Canonical Allele Identifier: CA2071351055
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs1954804506
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701658C>A , CM000674.2:g.128701658C>A GRCh38
NC_000012.11:g.129186203C>A , CM000674.1:g.129186203C>A GRCh37
NC_000012.10:g.127752156C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3432C>A MANE Select ENSP00000410852.2:n.2122-3432C>A
ENST00000435159.2:c.2122-3432C>A ENSP00000410852.2:n.2122-3432C>A
NM_001136103.2:c.2122-3432C>A NP_001129575.2:n.2122-3432C>A
XM_011538998.1:c.2062-3432C>A XP_011537300.1:n.2062-3432C>A
XM_011538998.2:c.2062-3432C>A XP_011537300.1:n.2062-3432C>A
XR_001748922.1:n.2355-2994C>A
NM_001136103.3:c.2122-3432C>A MANE Select NP_001129575.2:n.2122-3432C>A
NM_001387058.1:c.2062-3432C>A NP_001373987.1:n.2062-3432C>A
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